Oxidative Polymerization Research Articles

Preparation of environmentally responsive PDA&DOX@LAC live drug carrier for synergistic tumor therapy

The development of intelligent, environmentally responsive and biocompatible photothermal system holds significant importance for the photothermal combined therapy of tumors. In this study, inspired by Lactobacillus (LAC), we prepared a biomimetic nanoplatform PDA&DOX@LAC for tumor photothermal-chemotherapy by integrating the chemotherapeutic drug doxorubicin (DOX) with dopamine through oxidative polymerization to form polydopamine (PDA) on the surface of LAC. The PDA&DOX@LAC nanoplatform not only achieves precise and controlled release of DOX based on the slightly acidic microenvironment of tumor tissues, but also exhibits enzyme-like properties to alleviate tumor hypoxia. Under near-infrared light irradiation, it effectively induces photothermal ablation of tumor cells, enhances cellular uptake of DOX with increasing temperature, and thus efficiently inhibits tumor cell growth. Moreover, it is further confirmed in vivo experiments that photothermal therapy combined with PDA&DOX@LAC induces tumor cells apoptosis, releases tumor-associated antigens, which is engulfed by dendritic cells to activate cytotoxic T lymphocytes, thereby effectively suppressing tumor growth and prolonging the survival period of 4T1 tumor-bearing mice. Therefore, the PDA&DOX@LAC nanoplatform holds immense potential in precise tumor targeting as well as photothermal combined therapy and provides valuable insights and theoretical foundations for the development of novel tumor treatment strategies based on endogenous substances within the body.

Active films based on bio-polyethylene and natural extracts rich in tocopherols for food packaging applications

Antioxidant/antifungal active films based on bio-polyethylene (BPE) added with Nutrabiol®T90 and Tocobiol®Plus natural extracts rich in tocopherols at different concentrations (1 and 3 wt%) were developed by melt-blending followed by compression-molding. Thermal, barrier, mechanical, optical and functional properties of the developed active films were evaluated. The addition of active extracts did not cause important changes in thermal and barrier properties of active films whereas a significant increase in oxidative stability was found. Release kinetics of active additives migration showed higher tocopherol diffusion coefficient and antioxidant capacity, determined by the DPPH and ABTS methods, for films containing 3 wt% of Nutrabiol®T90. This film also delayed polymer oxidation in 260 min and extended strawberries shelf-life during storage for 7 days compared to neat BPE, showing a significant antifungal effect. The studied biomaterials offer great potential to substitute conventional petrol-derived materials at the industrial scale as active food packaging systems to increase the shelf-life of perishable foodstuff.

Facile Preparation of MXene Decorated PANI/Lignosulfonate Nanocomposite Film Electrodes for Electrochemical Supercapacitors

AbstractMXenes are a large family of two‐dimensional transition‐metal carbides, nitrides, and carbonitrides with large surface area and metal conductivity. They have not been widely used as electrodes in the field of supercapacitors because of their low specific capacity, poor chemical stability, and tendency towards self‐stacking. Herein, a three‐component nanocomposite film electrode has been successfully achieved, consisting of MXene nanosheets, polyaniline (PANI), and lignosulfonate (LGS). The PANI‐LGS nanocomposite was prepared through the oxidative polymerization of PANI in the presence of LGS, and then MXene decorated PANI/LGS (labeled as MPL) nanocomposite films were facilely self‐assembled via a vacuum‐assisted filtration by using the dispersion. Compared with pure PANI and PANI‐LGS, the MPL nanocomposite film electrode possesses better conductivity, showing a high specific capacitance of 559 F/g at a scan rate of 5 mV/s and a capacity retention rate of 92.2 % after 1000 cycles at a current density of 10 A/g. This study demonstrates that the doping of LGS and MXene can significantly improve the electrochemical performance of PANI‐based composite materials. Thus, the convenient preparation and excellent electrochemical performance of MPL show great potentials in the application of high‐performance electrodes for supercapacitors.

Electrochemical chiral sensor developed using nanofibrous polyaniline chiral Structures: Detection and differentiation of D- and L-tryptophan

In this work, a simple strategy for electrochemical detection and differentiation of D- and L- forms of tryptophan is demonstrated using nanofibrous structures of chiral polyaniline (CP). Basically, CP with desired chirality is prepared using a chiral acid namely, ± camphor sulfonic acid (±CSA) in presence of either a cationic (or) anionic surfactant (CTAB / SDS) through a simple oxidative polymerization process. Structure, morphology and phase purity of the resultant CP materials are characterized by field emission scanning electron microscopy, Fourier transform infrared spectroscopy, Raman spectroscopy and X-ray diffraction studies. Moreover, the chiral properties of these conducting polymers are evaluated using circular dichroism (CD) spectroscopic studies. From these analyses it is found that CP exhibited twisted nanofibrous morphology and possesses the chirality whereas the non-chiral polyaniline (PANI), prepared in the absence of chiral acid, displayed the formation of a simple fibrous structures without any twists or chirality. Interestingly, such CP materials are found to be electrochemically selective for the detection and differentiation of D- and L- forms of tryptophan (Trp). Among the different chiral materials, CP-CT(−) prepared using CTAB displayed a much better sensing characteristics with higher IL/ID ratio, wider concentration range of detection and lower detection limit of 0.98 µM for l-Trp and 1.2 µM for d-Trp respectively. On the other hand, non-chiral PANI does not display any sensing behavior towards the differentiation of amino acid, Trp. Further, chronoamperometric studies reveal the selectivity of this chiral sensor for the detection of Trp among the other potentially interfering analytes. Although the difference in the measured peak current value is smaller, a significant difference of 70 mV peak potential is observed for the differentiation of L- and d-Trp. Moreover, the proposed CP-based sensing platform exhibits excellent stability and reproducibility with statistically negligible error values suggesting the potential use of the developed material towards electrochemical chiral detection and differentiation of amino acid, Trp.

Soft modeling strategies at work to follow and rationalize dopamine oxidative polymerization

The role of dopamine (DA) oxidation in Parkinson’s disease makes to investigate the chemical aspects behind this process: in this paper, we applied Design of Experiments and Principal Component Analysis, to model the DA oxidative polymerization, unveiling the effect exerted by pH, ionic strength (I), temperature, and metal ions. Higher pH and T, lower I and Cu over Fe were found to result in faster DA consumption and smaller oligomers formation. We demonstrated that soft modelling strategies provide a valuable approach to deal with complex biochemical phenomena, regardless system complexity.

A Facile One-Step Self-Assembly Strategy for Novel Carbon Dots Supramolecular Crystals with Ultralong Phosphorescence Controlled by NH4.

A new methodological design is proposed for carbon dots (CDs)-based crystallization-induced phosphorescence (CIP) materials via one-step self-assembled packaging controlled by NH4 +. O-phenylenediamine (o-PD) as a nitrogen/carbon source and the ammonium salts as oxidants are used to obtain CDs supramolecular crystals with a well-defined staircase-like morphology, pink fluorescence and ultralong green room-temperature phosphorescence (RTP) (733.56ms) that is the first highest value for CDs-based CIP materials using pure nitrogen/carbon source by one-step packaging. Wherein, NH4 + and o-PD-derived oxidative polymers are prerequisites for self-assembled crystallization so as to receive the ultralong RTP. Density functional theory calculation indicates that NH4 + tends to anchor to the dimer on the surface state of CDs and guides CDs to cross-arrange in an X-type stacking mode, leading to the spatially separated frontier orbitals and the through-space charge transfer (TSCT) excited state in turn. Such a self-assembled mode contributes to both the small singlet-triplet energy gap (ΔEST) and the fast inter-system crossing (ISC) process that is directly related to ultralong RTP. This work not only proposes a new strategy to prepare CDs-based CIP materials in one step but also reveals the potential for the self-assembled behavior controlled by NH4 +.

Predicting mechanical heterogeneity in glassy polymer nanocomposites via an inverse computational approach based on atomistic molecular simulations and homogenization methods

Probing the mechanical behavior of the region formed between a nanoparticle reinforcement and a polymer matrix in a polymer nanocomposite structure, denoted as the “interphase”, is a main challenge as such regions are difficult to investigate by experimental methods. Here, we accurately characterize the heterogeneous mechanical behavior of polymer nanocomposites, focusing on polymer/nanofiller interphases via a combination of nanomechanical simulations and numerical homogenization techniques. Initially, the global mechanical performance of a glassy poly(ethylene oxide) polymer nanocomposite reinforced with silica nanoparticles is studied using detailed atomistic molecular dynamics simulations for 1.9% and 12.7% silica volume fractions. Next, the polymer/silica interphase thickness is identified by probing the polymer atom-based density distribution profile in the vicinity of the nanofiller at equilibrium. On the basis of this thickness, the interphase is subdivided to check the position-dependent change in mechanical properties. Then, using continuum mechanics and atomistic simulations, we proceed to compute the effective Young’s modulus and Poisson’s ratio of the polymer/nanoparticle interphase as function of the distance from the nanoparticle. In the last step, an inverse numerical homogenization model is proposed to predict the mechanical properties of the interphase on the basis of a comparison criteria with the data from MD. The results were found to be acceptable, raising the possibility of accurately and efficiently predicting interfacial properties in nanostructured materials.

Conjugated polymers decorated lignocellulosic nanocomposites for malachite green contaminated water remediation

Various novel conjugated polymer composites were synthesized via in situ chemical oxidative polymerization on lignocellulosic waste, notably Azadirachta indica sawdust. The composites, including Azadirachta indica/polyindole (AIS/PIn), Azadirachta indica/polyaniline (AIS/PAn), Azadirachta indica/polythiophene (AIS/PTh), and Azadirachta indica/polypyrrole (AIS/PPy), were investigated for their porous structure, ease of synthesis, unique adsorptive properties, and adjustable morphology. The synthesized composites were characterized using SEM/EDS, TEM/SAED, XRD, BET, TGA, and FTIR, revealing detailed insights into their structural and morphological features. The potential of these composites as efficient adsorbents for removing malachite green (MG) dye from water was a vital focus of this research. Batch experiments were conducted to assess the impact of various factors on adsorption, such as adsorbent/adsorbate contact time (0–280 min.), adsorbent dosage (0.4–20.0 g/L), initial adsorbate concentration (25–100 ppm), pH (2–13), and temperature (30–60 °C). The results indicate a remarkable removal efficiency of 89.98 % for MG with an initial concentration (Co) of 50 mg/L, achieved within 120 min using 0.4 g/L of AIS/PIn at a pH above 8.3. The Langmuir adsorption isotherm model provided the best fit for the experimental data, with maximum adsorption capacities of 384.61 mg g−1 for AIS/PIn, 344.82 mg g−1 for AIS/PAn, 277.77 mg g−1 for AIS/PTh, and 256.41 mg g−1 for AIS/PPy. This suggests monolayer adsorption. The adsorption kinetics conformed to a pseudo-second-order model, with the process being endothermic, feasible, and associated with positive entropy, thereby underlining its favorability and spontaneity. The desorption studies determined that 0.1 M HCl was the most effective desorbing agent compared to NaOH, NaCl, CH3COOH, and H2O. The spectral and effect of pH analyses suggested that the adsorption mechanisms might involve multiple interactions, prominently including electrostatic interactions, hydrogen bonding, π-π interactions, and n-π interactions. Based on the findings, it is submitted that the conjugated polymer decorated biomass composite adsorbents exhibit reasonable recyclability over multiple cycles, versatility, and potent efficacy as low-cost adsorbents for eliminating MG dye from aqueous systems.

Expansion of Auxiliary Activity Family 5 sequence space via biochemical characterization of six new copper radical oxidases.

Bacterial and fungal copper radical oxidases (CROs) from Auxiliary Activity Family 5 (AA5) are implicated in morphogenesis and pathogenesis. The unique catalytic properties of CROs also make these enzymes attractive biocatalysts for the transformation of small molecules and biopolymers. Despite a recent increase in the number of characterized AA5 members, especially from subfamily 2 (AA5_2), the catalytic diversity of the family as a whole remains underexplored. In the present study, phylogenetic analysis guided the selection of six AA5_2 members from diverse fungi for recombinant expression in Komagataella pfaffii (syn. Pichia pastoris) and biochemical characterization in vitro. Five of the targets displayed predominant galactose 6-oxidase activity (EC 1.1.3.9), and one was a broad-specificity aryl alcohol oxidase (EC 1.1.3.7) with maximum activity on the platform chemical 5-hydroxymethyl furfural (EC 1.1.3.47). Sequence alignment comparing previously characterized AA5_2 members to those from this study indicated various amino acid substitutions at active site positions implicated in the modulation of specificity.IMPORTANCEEnzyme discovery and characterization underpin advances in microbial biology and the application of biocatalysts in industrial processes. On one hand, oxidative processes are central to fungal saprotrophy and pathogenesis. On the other hand, controlled oxidation of small molecules and (bio)polymers valorizes these compounds and introduces versatile functional groups for further modification. The biochemical characterization of six new copper radical oxidases further illuminates the catalytic diversity of these enzymes, which will inform future biological studies and biotechnological applications.

Enhancing Photocathodic Performances of Particulate-CuGaS2-Based Photoelectrodes via Conjugation with Conductive Organic Polymers for Efficient Solar-Driven Hydrogen Production and CO2 Reduction.

Modification with conductive organic polymers consisting of a thiophane- or pyrrole-based backbone improved the cathodic photocurrent of a particulate-CuGaS2-based photoelectrode under simulated solar light. Among these polymers, poly(3,4-ethylenedioxythiophene) (PEDOT) was the most effective in the improvements, providing a photocurrent 670 times as high as that of the bare photocathode. An incident-photon-to-current efficiency (IPCE) for water reduction to form H2 under monochromatic light irradiation (450 nm at 0 V vs RHE) was ca. 11%. The most important point is that modification of the conductive organic polymers does not involve any vacuum processes. This importance lies in the use of an electrochemically oxidative polymerization, not in a physical process such as vapor deposition of metal conductors. This is expected to be advantageous in the large-scale application of photocathodes consisting of particulate photocatalyst materials toward industrial solar-hydrogen production using photoelectrochemical-cell-based devices. Artificial photosynthesis of water splitting and CO2 reduction under simulated solar light was demonstrated by combining the PEDOT-modified CuGaS2 photocathode with a CoOx-loaded BiVO4 photoanode. Furthermore, how the cathodic photocurrent of the particulate-CuGaS2-based photocathode was drastically improved by the modification was clarified based on various characterizations and control experiments as follows: (1) selectively filling cavities between the particulate CuGaS2 photocatalysts and a conductive substrate (FTO; fluorine-doped tin oxide) with the polymers and (2) using a large driving force for carrier transportation governed by the polymers' redox potentials adjusted by functional groups.

Polypyrrole modified MIL-101-Fe-derived Fe/Fe3O4@C composites for high-performance microwave absorber

Carbon-based microwave absorbing composites with magnetic-dielectric properties and multiple loss mechanism are considered to be an effective choice for solving electromagnetic pollution. In this paper, the PPy/Fe/Fe3O4@C composite was synthesized from MIL-101-Fe derivatives and subsequently coated polypyrrole (PPy) by combining hydrothermal, high-temperature pyrolysis and oxidative polymerization. The effects of pyrolysis temperature and PPy loading on components, microstructures and electromagnetic parameters were investigated. The results showed that the PPy/Fe/Fe3O4@C composite consisted of two-dimensional carbon flakes modified by magnetic particles and laminated conductive polymers. When the PPy loading is moderate, the composite reaches a minimum reflection loss (RLmin) of −61.38 dB at a 3.1 mm thickness and effective absorption bandwidth (EAB) of 5.81 GHz at the thickness of 2.2 mm. After pyrolysis, the unique three-dimensional structure of carbon sheet stacking, as well as the heterogeneous interface and conductive networks generated by the modification of magnetic particles Fe and Fe3O4 and conductive PPy, are beneficial to improve the dielectric and magnetic losses to optimize the impedance matching. These conductive polymer-modified magnetic-dielectric composites have potential for development and application in microwave absorption.

Study on Bonding Characteristics of Aluminum Alloy Treated by Plasma Electrolytic Oxidation Process and Polymer Resin Bonded by Direct Injection Molding

Aluminum alloy and polymer resin hybrid bonding technology is essential for lightweight mobile phone frames and automotive components. Recently, there has been extensive research on a method of bonding metals and polymer resins by treating the metal surface and then direct injection molding. However, this method requires separate surface treatment of the aluminum alloy after bonding to enhance its corrosion resistance. This paper studies the use of Plasma Electrolytic Oxidation, one of the surface treatment methods for aluminum, to achieve the bonding of aluminum and polymer resin in a single surface treatment step while ensuring high corrosion resistance. We conducted research to investigate optimal conditions by adjusting the process variables of Plasma Electrolytic Oxidation, in order to achieve integration with the polymer resin and measure the bonding strength and corrosion resistance. The surface characteristics of each Plasma Electrolytic Oxidation condition were analyzed using scanning electron microscopy and atomic force microscope equipment, while the bonding strength was measured using universal testing machine equipment. The corrosion characteristics were evaluated by measuring the corrosion resistance in a saltwater solution.

Elucidating the role of Ag+, Cu2+, and Fe3+ in tuning the electrical characteristics of polyaniline prepared through post-doping method

Abstract Conducting polymers possess inherent electrical conductivity, attracting significant attention in engineering applications, including dye-sensitized solar cells, gas sensors, and energy storage electrodes. Of various conducting polymers, Polyaniline has gained much attention due to its low cost of monomer, ease of bulk synthesis, high flexibility, and good environmental stability. Nevertheless, the conductivity of polyaniline is rather low when it is prepared under an un-doped state. Despite that, there is no clear information regarding how the valency of a metal dopant and its concentration can affect the electrical characteristics and other physicochemical properties of doped polyaniline. This study aims to fill this research gap by elucidating the changes in the electrical characteristics of polyaniline through metal doping. Polyaniline was synthesized through chemical oxidative polymerization in an HCl medium, followed by a post-doping to produce metal-codoped polyaniline. Three dopant materials, namely AgNO3, Cu(NO3)2, and Fe(NO3)3, were used in this synthesis, representing mono-, di-, and tri-valent metal ions, respectively. Results showed that bare PANI (which was doped with HCl only) exhibited a higher electrical conductance value of 8.44 x 10-7 S, while 1 M of Ag-codoped polyaniline, 1 M of Cu-codoped polyaniline, and 1 M of Fe-codoped polyaniline exhibited electrical conductance values of 1.73 x 10-7 S, 4.27 x 10-8 S, and 2.33 x 10-6 S, respectively. Apparently, the trivalent metal dopant was able to improve the conductivity of polyaniline; however, a detrimental effect resulted when the concentration of Fe3+ was increased to 1.5 M (overdose), resulting in a drop in electrical conductance to 4.66 x 10-8 S. In terms of morphological property, Ag-doped polyaniline exhibited a mixture of plate-like and globule-like structures, while both Cu-doped polyaniline and Fe-doped polyaniline predominantly displayed tiny globule-like structures, likely attributed to the stronger acidity of the Cu(NO3)2 and Fe(NO3)3 solutions. Meanwhile, the presence of several common bands of polyaniline such as N-H, C=N, C-H aromatic, quinoid and benzoid units are detected in the produced samples. The project outcomes are expected to guide tailored development of metal-doped polyaniline for specific electrical applications.

Non-uniform polarization boosted electromagnetic wave absorption with high efficiency and a broad frequency range

3-Aminobenzene sulfonic acid (mASA) has been co-polymerized into polyaniline (PANI) surface layers of ferrite nano particles by oxidative polymerization method. The sulfonic group of mASA anchored into PANI molecular have been employed as a dopant of PANI to partially substitute the dissociative dopant, hydrochloric acid (HCl). Owing to the constrained local distribution of mASA in PANI, the non-uniform polarization of PANI has been successfully stimulated by sulfonic acid doping. This results in various scattering loss modes and refined impedance matching in the synthesized ferrite/PANI nano-composite, which contributes to excellent absorbing properties with a high reflection loss of −56.42 dB and a broad effective absorption bandwidth of 3.8 GHz. The exhibited performances in microwave absorption are superior to most of ferrite-related composites. The explored strategy provides a novel way to tailor microwave absorbing composites to enhance their comprehensive microwave absorbing properties.

Conjugated diacetylene polymers with intrachain D-A block heterostructure for efficient photocatalytic hydrogen production

Solar-driven photocatalytic hydrogen production has been considered as a promising candidate technology for supplying green and sustainable energy source alternative to fossils. But its low solar-to-hydrogen conversion efficiency level hampers its practical application, and lack of effective structure for promoting charge separation is one of the accounts. Herein, intrachain heterojunction structure comprised of donor-acceptor (D-A) blocks has been proved to be one of effective structures for addressing such an issue. Utilizing the facile oxidative coupling polymerization reactions of diacetylene monomers and oligomers, a block heterojunction polymeric photocatalyst named PDTPDPA-BP bearing D-A blocked heterostructure was synthesized by first separative oligomerizations of diacetylene-functionalized dibenzothiophene sulfone (DTP) and triphenylamine (TPA) monomers and then mixed together and undergoing further polymerization. In photocatalytic hydrogen production, PDTPDPA-BP displayed a hydrogen evolution rate of 2164 μmol g−1 h−1, which is much larger than those of PDTP (1270 μmol g−1 h−1) and PTPA (57 μmol g−1 h−1) synthesized by homopolymerization of DTP and TPA monomers, respectively, and their 1:1 molar ratio physical blend (363 μmol g−1 h−1). By means of Fluorescence spectroscopy and photo-responsive measurements, it was found PDTPDPA-BP has narrower bandgap and more efficient charge separation than the other polymers. Therefore, the work highlights intrachain heterojunction structure promotes exciton dissociation into free charge carries, and thus deserves the consideration in the design of high performance organic photocatalysts.

Enhanced performance of Lagerstroemia speciosa seed biochar and polypyrrole composite for the sequestration of emerging contaminant from wastewater sample: Case study of ofloxacin drug

Pharmaceutical effluents containing fluroquinolones (FQs) are one of the incipient organic impurities in aquatic environment. The ecosystem and human health were seriously affected from the remaining FQs in marine environment because of their toxicity. Hence, elimination of this FQs by emerging adsorbents with higher efficacy needs to be developed. This current research intends to developed a novel chemically modified jarul biochar/polypyrrole (CLSHB/PPy) composite via pyrolysis followed by sodium hydroxide modification and oxidative polymerization of pyrrole monomer to sequestrate ofloxacin (OFX) from aqua matrix. The characterization results of fabricated composite revealed that agglomerated spherical shape particles and their crystallinity nature can be act as an adequate adsorbent. Several sorption progression limitations are optimized which impact the interaction between CLSHB/PPy and OFX species. The optimum OFX eradication (%) of 82.42 ± 0.90 % by CLSHB/PPy was detected at pH 7.0, dose 1.0 g/L, and initial concentration 60 mg/L. Furthermore, Langmuir isotherm exhibited well fitted (R2 = 0.99) investigational data with an elimination ability of 50.02 ± 0.65 mg/g. Besides, kinetic analysis exposed that Pseudo second order model contribute the best suited kinetic. Thermodynamic study revealed that sorption progression of OFX onto CLSHB/PPy was both spontaneous and endothermic (∆H° ˃ 0). Moreover, CCD optimization exposed that investigational outcome (84.81 ± 1.02 %) are also adjacent to model integrated outcomes (84.12 ± 0.85 %), which indicates importance of RSM analysis. Stability analysis of composite (CLSHB/PPy) has been executed and exposed that the composite material can be effectively reutilized for OFX sorption after certain cycles.

Hybrid Nanocomposites Based on Poly(3,6-dianiline-2,5-dichloro-1,4-benzoquinone): Synthesis, Structure and Properties.

Hybrid nanocomposites based on poly(3,6-dianiline-2,5-dichloro-1,4-benzoquinone) (PDACB) in salt form and graphene oxide (GO) have been obtained for the first time, and the significant influence of the preparation method on the composition and structure of nanocomposites and their functional properties has been demonstrated. Nanocomposites were prepared in three ways: via ultrasonic mixing of PDACB and GO; via in situ oxidative polymerization of 3,6-dianiline-2,5-dichloro-1,4-benzoquinone (DACB) in the presence of GO; and by heating a suspension of previously prepared PDACB and GO in DMF with the removal of the solvent. The results of the study of the composition, chemical structure, morphology, thermal stability and electrical properties of nanocomposites obtained via various methods are presented. Nanocomposites obtained by mixing the components in an ultrasonic field demonstrated strong intermolecular interactions between PDACB and GO both due to the formation of hydrogen bonds and π-stacking, as well as through electrostatic interactions. Under oxidative polymerization of DACB in the presence of GO, the latter participated in the oxidative process, being partially reduced. At the same time, a PDACB polymer film was formed on the surface of the GO. Prolonged heating for 4 h at 85 °C of a suspension of PDACB and GO in DMF led to the dedoping of PDACB with the transition of the polymer to the base non-conductive form and the reduction of GO. Regardless of the preparation method, all nanocomposites showed an increase in thermal stability compared to PDACB. All nanocomposites were characterized by a hopping mechanism of conductivity. Direct current (dc) conductivity σdc values varied within two orders of magnitude depending on the preparation conditions.

Enhancing electron transfer in anaerobic process by supercapacitor materials: Polyaniline functionated activated carbon

Strengthening the direct interspecies electron transfer (DIET) is an effective strategy to improve the performance of anaerobic digestion (AD) process. In this study, the polyaniline functionated activated carbon (AC-PANi) was prepared by chemical oxidative polymerization. This material possessed pseudo-capacitance properties as well as excellent charge transfer capability. The experimental results demonstrated that the incorporation of AC-PANi in AD process could efficiently increase the chemical oxygen demand (COD) removal (18.6 %) and daily methane production rate (35.3 %). The AC-PANi can also act as an extracellular acceptor to promote the synthesis of adenosine triphosphate (ATP) and secretion of extracellular enzymes as well as cytochrome C (Cyt-C). The content of coenzyme F420 on methanogens was also shown to be increased by 60.9 % with the addition of AC-PANi in AD reactor. Overall, this work provides an easy but feasible way to enhance AD performance by promoting DIET between acetate-producing bacteria and methanogens.

Silver@copper-polyaniline nanotubes: Synthesis, characterization and biosensor analytical study

We introduce silver-copper nanoparticles incorporated into polyaniline (PANI) nanotubes using a straightforward and efficient reduction process. In this regard, PANI nanotubes with amine groups were fabricated through oxidation polymerization, followed by the attachment of Ag and Cu precursors to enable the synthesis of Ag-Cu bimetallic nanoparticles (NPs) on the pre-formed PANI nanotubes with the use of hydrazine as a reducing agent. The structural characterization of the synthesized NPs was investigated by UV–Vis spectrophotometer (UV–Vis), Dark-field emission, (EDX), X-ray diffraction (XRD) and field emission (FESEM), while the electrochemical properties were estimated by (CV) and differential pulse voltammetry (DPV). The findings indicated that the Ag-Cu NPs were present in the nanoscale range, well-dispersed, and attached to the surface of PANI nanotubes. Electrochemical investigations revealed that the Ag-Cu@PANI nanotube electrode demonstrated efficient electrooxidation of dopamine and hydroquinone without any interfering reactions, suggesting its potential use as an electrochemical biosensor for simultaneous detection of dopamine and hydroquinone. The proposed NPs-based biosensor was connected to concurrently identify dopamine and hydroquinone, illustrating moo distinguish Confinements of 0.46 µM for dopamine and 0.23 mM for hydroquinone, separately. Additionally, the manufactured sensor identified on a wide direct run the dopamine (5–25 µM), and hydroquinone (0.5–2.5 mM). Alongside these promising comes about, the Ag-Cu@PANI nanotube actualized great solidness and reproducibility, making it a favorable stage for electrochemical biosensing of dopamine and hydroquinone.

Conducting Carbon Black Nano‐Filler Doped Polymer Electrolyte for Electrochemical Application

AbstractThis study provides a development of polymer electrolytes with an emphasis on their use in electrochemical devices. In present study we develop a new conducting carbon black (CB) powder dispersed into polyethylene oxide (PEO) polymer electrolyte using solution cast method. Various characterization techniques such as Impedance spectroscopy technique (EIS), Fourier transform infrared spectroscopy (FTIR), and Window stability (LSV) Linear sweep voltammetry has been studied in detail. The maximum ionic conductivity polymer electrolyte was at 0.05 wt%. of CB with σ value 1.20×10−5 S/cm. Finally the prepared CB dispersed polymer electrolyte using maximum conductivity sample is sandwiched between electrodes to fabricate an Electric double layer capacitor and Dye‐sensitized solar cell which show highest electrical capacity value of 68.5 F/gm at 5 mV/s respectively and 2.97 % efficiency shown by solar cell at 1 sun condition.